Combinatorial approaches that leverage translationally relevant behavior and
neuroanatomy can be used to develop a platform for assessment of cutting edge preclinical …

Prader–Willi syndrome (PWS), a rare epigenetic disease mapping the imprinted
chromosomal domain of 15q11. 2-q13. 3, manifests a regular neurodevelopmental trajectory …

Background Responding to social signals by expressing the correct behavior is not only
challenged in autism but also in diseases with a high prevalence of autism, such as Prader …

The objective of this study was to investigate lobule-specific cerebellar structural alterations
relevant to clinical behavioral characteristics of Prader-Willi syndrome (PWS). We performed …

Introduction Obesity has become a global public health issue, which impacts general health
and the brain. Associations between obesity and white matter microstructure measured …

Ultra-high field magnetic resonance imaging (MRI) has been introduced for use in pediatric
developmental neurology. While higher magnetic fields have certain advantages, optimized …

Background: Prader–Willi syndrome (PWS) is a genetic syndrome with clinical behavioral
phenotypes, including autistic characteristics. However, brain functional connectivity (Fc) …

Abstract Prader-Willi syndrome (PWS), a congenital genetic disorder, has received attention
due to its features, including hyperphagic behavior with a unique genetic background. While …

Prader-Willi syndrome (PWS) is a is a pervasive neurodevelopmental syndrome with a
characteristic behavior profile that includes a typical yet abnormal food-related behavior …

Introduction Corpus callosotomy (CC) is an established surgical option for palliative
treatment of medically intractable epilepsy, especially for seizures with drop attacks. We …